Product Recalls in Florida

Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,206 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,206 in last 12 months

Showing 981–1000 of 30,686 recalls

Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 Recalled by Olympus Corporation of the...

The Issue: Additional IFU updates to provide further clarification on safe and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: LGX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...

The Issue: The potential for devices to experience inflation and/or deflation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 Recalled by Olympus Corporation of the...

The Issue: Additional IFU updates to provide further clarification on safe and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: LGX Preconnect with TENACIO Pump with InhibiZone Recalled by Boston...

The Issue: The potential for devices to experience inflation and/or deflation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2025· Medline Industries, LP

Recalled Item: Medline Adult Anesthesia Set Recalled by Medline Industries, LP Due to...

The Issue: Specific items and lots of Medline Kits may contain Clearlink IV Sets which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2025· Draeger, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500...

The Issue: The device either indicated a failure of the piston ventilator before use or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 9, 2025· Draeger, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600...

The Issue: The device either indicated a failure of the piston ventilator before use or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 9, 2025· Biomet, Inc.

Recalled Item: Juggerknot Mini Soft Anchors Recalled by Biomet, Inc. Due to The outer...

The Issue: The outer carton box label is for the JuggerKnot 1.0mm Mini products....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2025· MedicalCommunications GmbH

Recalled Item: Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version Recalled by...

The Issue: Potential that the measured value may be smaller than the actual area.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 6" (15 cm) Ext Set w/MicroClave" Clear Recalled by ICU Medical,...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Oncology Kit w/31" (79 cm) 20 Drop Admin Recalled by ICU...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock w/Mini Bag Spike ¿ Recalled by ICU Medical, Inc. Due...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 73" (185 cm) Appx 2.5 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock 13mm Closed Vial Spike Recalled by ICU Medical, Inc....

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 8" (20 cm) Ext Set w/MicroClave Clear Recalled by ICU Medical,...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 31" (79 cm) Appx 3.4 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Closed Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Oncology Kit w/ChemoLock Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Clave Bag Spike w/ChemoLock Port Recalled by ICU Medical, Inc....

The Issue: Port weld of drug transfer device may separate or break during use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing